Rollin with Rollie - Same Game Same Rules

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Rollin with Rollie - Same Game Same Rules I roll ♿ and I bowl 🎳
Same game, same rules. No exceptions. Advocacy through every frame. 📍 Indiana
Join the journey! 👇

Tonight was a solid incline from last week's scores. Finished tonight with games of 122, 114, and 101, beating out my cu...
10/13/2026

Tonight was a solid incline from last week's scores. Finished tonight with games of 122, 114, and 101, beating out my current 102 Monday night average.

• Game 1 (122): Opened up shaky, but bounced back with a double. Hit the pocket consistently and just endured a few bad breaks.

• Game 2 (114): The pocket hits were there, but the carry wasn't. Ended up with just a single strike.

• Game 3 (101): Lost my consistency here, pulling shots left and missing right. Thankfully, a few lucky spares salvaged the score.

Not a perfect night, but definitely a much-needed improvement!

I hadn't planned on making a post about any of my pictures specifically, but after a few people asked me about the one t...
10/09/2026

I hadn't planned on making a post about any of my pictures specifically, but after a few people asked me about the one that happens to be my favorite, I figured it was time to talk about it.

There's a reason I edited this picture differently than the others, and it goes a lot deeper than most people would ever imagine.

Being a wheelchair user is hard enough on its own. Now add being a wheelchair user who bowls in a tiny-ass town with an eight-lane bowling center. There wasn't exactly a roadmap for me to follow. No one had laid out the path ahead of me. I had to figure things out as I went and pave my own way.

Thankfully, I had able-bodied people willing to teach me, support me, and help me grow. Throughout my bowling journey, I've always bowled with and against able-bodied bowlers. That's what I knew. That's the environment I grew up in, and for a long time, it was the only environment I knew.

But here's the part that still blows my mind.

I was 22 years old before I ever bowled with or against another wheelchair user.

I'm only 23 now. I've been bowling for 10 years, and it took nearly that entire journey before I finally competed against someone else who understood that part of my experience firsthand.

Let that sink in.

For years, I competed in a sport I loved without having someone on the other side of the lanes who could truly relate to what it was like to experience that sport from a wheelchair. Someone who understood the adjustments, the challenges, and the little things that most people never have to think twice about.

And that means more than I think some people realize.

So, when I edited this picture, I wanted to do something different. Something a little abnormal. Something that stood out.

Because, in a lot of ways, that's what I've had to do my entire life.

I've had to learn differently, adapt differently, and find my own way in spaces that weren't necessarily built with people like me in mind. I've had to figure things out without always having someone who understood what it was like to be in my shoes - or in my wheels.

I've had to learn by doing, make adjustments along the way, and keep pushing forward even when there wasn't anyone ahead of me showing me exactly how it could be done.

And no, this isn't about feeling sorry for myself. Not even a little bit.

It's about recognizing how far I've come. It's about appreciating the people who believed in me, taught me, and helped me get to where I am today. And it's about understanding that sometimes, your journey looks different simply because there isn't a path waiting for you to follow.

Sometimes, you have to create the path yourself.

Sometimes, you have to be the first person in the room, the first person on the lanes, or the person doing something differently because that's what works for you. Sometimes, you have to become the example you spent years wishing you could see.

And maybe that's one of the most meaningful parts of this entire journey.

Because if my experiences in bowling and in life can make the road a little less intimidating for the next wheelchair user who wants to roll onto those lanes, then every challenge, every adjustment, every frustrating moment, and every ounce of work I've put into this will mean that much more.

Maybe the next wheelchair bowler won't have to wait until they're 22 to compete against someone who understands their experience.

Maybe they'll have someone to look up to, someone to learn from, or simply someone who makes them realize they're not the only one out there.

And if I can help make that happen, even in a small way, then I know I'm doing something that matters.

I may not have had someone paving the way for me, but that doesn't mean I can't help pave the way for someone else.

That's what this picture means to me. And that's why it's my favorite. 🎳♿

I regularly have people come up to me and tell me that they think it's cool or awesome that I go out and do the things I...
10/08/2026

I regularly have people come up to me and tell me that they think it's cool or awesome that I go out and do the things I do with my able-bodied peers and I know I usually have to a pretty plain response to them but I really do appreciate all of the support. Sometimes I'm just mentally or physically exhausted because it's not easy but it dang sure is possible 💪

Bowling is more than throwing a ball down a lane. It’s focus, patience, strategy, confidence, and the determination to k...
10/08/2026

Bowling is more than throwing a ball down a lane. It’s focus, patience, strategy, confidence, and the determination to keep going shot after shot. 🎳

From the preparation, to the release, to watching those pins fall - every moment is part of the game. These photos capture more than a day at the bowling alley; they capture the passion, personality, and competitive spirit behind every roll.

The lane doesn’t care how you get there. It’s about showing up, trusting yourself, and giving the next shot everything you’ve got. 🎳🔥

One bowler. One ball. One lane. Endless possibilities

10/03/2026

Thank you Tiffany Denham and Cody Denham for trying this out today!

October is Spina Bifida Awareness Month, and I am celebrating by being exactly who I’ve always been: Unapologetically ME...
10/03/2026

October is Spina Bifida Awareness Month, and I am celebrating by being exactly who I’ve always been: Unapologetically ME.
I have Spina Bifida Myelomeningocele (pronounced my-low-ma-nin-jo-seal). Spina Bifida Myelomeningocele is a birth defect where a baby’s backbone and spinal cord do not close properly before birth, leaving a fluid-filled sac of exposed nerves sticking out of their back.
To break down the medical jargon, think of it like this:
• Spina Bifida: Literally means "split spine". The bones of the backbone fail to form a solid, protective ring around the spinal cord.
• Myelomeningocele: This is the most severe and common type of spina bifida. "Myelo" means spinal cord, and "meningocele" means a swelling of the protective membranes.
Because the spine stays open, a small sac pushes out through the gap in the baby's back. This sac contains cerebrospinal fluid, protective membranes, and crucial nerve tissue. Because those nerves are unprotected and exposed to the environment inside the womb, they get damaged.
Why does it happen?
Doctors don't know the exact single cause, but it happens in the first month of pregnancy—often before a person even knows they are pregnant. It is heavily linked to a lack of folic acid (a vital B vitamin) in the parent's diet, alongside certain genetic and environmental triggers.
How does it affect a person?
Because the nerves in the sac are damaged, the brain cannot send or receive signals properly past that point in the spine. It usually results in:
• Mobility issues: Weakness or complete paralysis in the legs, often requiring braces, crutches, or a wheelchair.
• Bladder and bowel control issues: The nerves controlling these functions are almost always affected.
• Fluid buildup in the brain (Hydrocephalus): The spinal opening can disrupt how brain fluid drains, requiring a small tube (shunt) to be surgically put in to drain the extra fluid.
How is it treated?
There is no cure for the nerve damage, but doctors usually perform surgery to close the opening in the back. This surgery can happen shortly after birth, or in some cases, specialized teams can even perform Fetal Surgery while the baby is still inside the womb to protect the nerves from further damage. People with this condition usually work with a lifelong team of doctors to help them live active, independent livesBut that's just a medical term - it don't define my limits, and it sure as hell don't stop me from doing something I want do.
Growing up I was always raised knowing that I had to try to do something for myself before I asked for helped. Did that mean I could do everything for myself? Absolutely not! And I still can't. That's just the reality of having the medical issues that I do have. But, it helped me realize I can do much more in this world that I would have ever thought possible if I hadn't been raised the way I was.
Case in point - from my wheelchair, I still do what I want, when I want, and how I want. I've proven that by:
• Learning to walk with as little as a single crutch before transitioning to my chair full-time at 17
• Conquering both a 5K and a 4-mile race in my wheelchair
• Dominating the bowling lanes as a dedicated wheelchair bowler for 10 years and counting 🎳
Those are just 3 things I've done in my life. I've accomplished so much more than I honestly probably even remember. I'm out here living life loud, breaking molds, and rolling through every barrier in my way. ♿⚡

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Versailles, IN
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